Density Functional Theory of the Electrical Conductivity of Molecular Devices

Kieron Burke, Roberto Car, and Ralph Gebauer
Phys. Rev. Lett. 94, 146803 – Published 13 April 2005; Erratum Phys. Rev. Lett. 94, 159901 (2005)

Abstract

Time-dependent density functional theory is extended to include dissipative systems evolving under a master equation, providing a Hamiltonian treatment for molecular electronics. For weak electric fields, the isothermal conductivity is shown to match the adiabatic conductivity, thereby recovering the Landauer result.

  • Received 14 October 2004
  • Publisher error corrected 15 April 2005

DOI:https://doi.org/10.1103/PhysRevLett.94.146803

©2005 American Physical Society

Corrections

15 April 2005

Erratum

Authors & Affiliations

Kieron Burke1, Roberto Car2, and Ralph Gebauer3,4

  • 1Department of Chemistry and Chemical Biology, Rutgers University, 610 Taylor Road, Piscataway, NJ 08854, USA
  • 2Department of Chemistry and Princeton Institute for the Science and Technology of Materials (PRISM), Princeton University, NJ 08544, USA
  • 3The Abdus Salam International Centre for Theoretical Physics (ICTP), 34014 Trieste (Italy)
  • 4INFM/Democritos, National Simulation Center, 34013 Trieste, Italy

Article Text (Subscription Required)

Click to Expand

References (Subscription Required)

Click to Expand
Issue

Vol. 94, Iss. 14 — 15 April 2005

Reuse & Permissions
Access Options
Author publication services for translation and copyediting assistance advertisement

Authorization Required


×
×

Images

×

Sign up to receive regular email alerts from Physical Review Letters

Log In

Cancel
×

Search


Article Lookup

Paste a citation or DOI

Enter a citation
×